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Anti stim1 antibody

Manufactured by Abcam
Sourced in United States

The Anti-STIM1 antibody is a laboratory tool used to detect and study the STIM1 protein. STIM1 is a calcium sensor that plays a key role in the regulation of cellular calcium homeostasis. This antibody can be used in various techniques such as Western blotting, immunohistochemistry, and immunocytochemistry to analyze the expression and localization of STIM1 in different biological samples.

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2 protocols using anti stim1 antibody

1

TGF-β Signaling and Calcium Regulation

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All cell lines used in this work were obtained from American Type Culture Collection (Manassas, VA, USA). Cells were cultured as we previously described [42 (link)].
TGF-β was purchased from R&D systems (Minneapolis, MN, USA). SKF96365 was bought from Abcam (Abcam, UK). The calcium dye Fura 2-AM and EGTA were obtained from Invitrogen (Carlsbad, CA, USA). The antibodies against ERK1/2, p-ERK1/2 were bought from Bioworld Technology (Louis Park, MN, USA) and anti-STIM1 antibody was from Abcam (Abcam, UK). The anti-GAPDH antibody was bought from KANGCHEN BIO-TECH (Shanghai, China). HRP-conjugated goat anti-rabbit antibody was purchased from Thermo Scientific (Waltham, MA, USA).
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2

Analyzing STIM1 and ORAI1 in Bone Marrow Megakaryocytes

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To analyze STIM1 and ORAI1 in BM Mks, femurs were flushed, and red blood cells were lysed with 0.8% ammonium chloride solution. The remaining cells were washed by centrifugation with phosphate-buffered saline and stained with anti-ORAI1 antibody (1:100; Santa Cruz Biotechnologies) or anti-STIM1 antibody (1:100; Abcam). For STIM1 staining, cells were permeabilized with commercial buffers (BD Pharmingen) prior to staining with the antibody. To recognize BM Mks, we costained cells with an anti-CD41 antibody (0.1 mg/mL; BioLegend). All Mk samples were characterized as CD41/CD42b-positive and CD3/CD4/CD8/CD11b/CD19/CD33-negative cells, using appropriate antibodies (0.1 mg/mL; all from Beckman Coulter). Samples were acquired with a FACSDiva flow cytometer (Beckman Coulter). The analytical gating was set using unstained samples and relative isotype controls. Offline data were analyzed using the Beckman Coulter Kaluza software package (Beckman Coulter) and Flowing software 2.5.1 (University of Turku).
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